Identity
HGNC
LOCATION
6p12.3
LOCUSID
ALIAS
CD241,OHS,OHST,RH2,RH50A,RHNR,Rh50,Rh50GP,SLC42A1
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 6005
MIM: 180297
HGNC: 10006
Ensembl: ENSG00000112077
Variants:
dbSNP: 6005
ClinVar: 6005
TCGA: ENSG00000112077
COSMIC: RHAG
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38711255 | 2024 | Rh(null) phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene. | 0 |
| 38711255 | 2024 | Rh(null) phenotype in an Indian patient due to a novel c.1138 + 2 t > a mutation in the RHAG gene. | 0 |
| 32378229 | 2020 | Extensive clinical, serologic and molecular studies lead to the first reported Rh(mod) phenotype in Argentina. | 0 |
| 32705675 | 2020 | The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn. | 2 |
| 32378229 | 2020 | Extensive clinical, serologic and molecular studies lead to the first reported Rh(mod) phenotype in Argentina. | 0 |
| 32705675 | 2020 | The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn. | 2 |
| 29508504 | 2019 | A RHAG point mutation selectively disrupts Rh antigen expression. | 1 |
| 30990901 | 2019 | Rh(null) phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population. | 0 |
| 31032541 | 2019 | A novel double-variant RHAG allele leads to Rh(mod) phenotype. | 0 |
| 29508504 | 2019 | A RHAG point mutation selectively disrupts Rh antigen expression. | 1 |
| 30990901 | 2019 | Rh(null) phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population. | 0 |
| 31032541 | 2019 | A novel double-variant RHAG allele leads to Rh(mod) phenotype. | 0 |
| 29266289 | 2018 | A novel nucleotide deletion in RHAG allele identified in a Chinese Rh(null) individual. | 0 |
| 29559519 | 2018 | Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation. | 0 |
| 29266289 | 2018 | A novel nucleotide deletion in RHAG allele identified in a Chinese Rh(null) individual. | 0 |
Citation
Dessen P
RHAG (Rh associated glycoprotein)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/72622/rhag-(rh-associated-glycoprotein)
